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The Cystic Fibrosis Transmembrane Conductance Regulator 470 Met Allele Is Associated with an Increased Risk of Chronic Pancreatitis in Both Asian and Caucasian Populations: A Meta-Analysis.
Genetic Testing and Molecular Biomarkers ( IF 1.4 ) Pub Date : 2020-01-01 , DOI: 10.1089/gtmb.2019.0199
Donger Zhou 1 , Rui Bai 2 , Liang Wang 1
Affiliation  

Background: The Met470Val polymorphism (1540A>G [rs213950]) within the cystic fibrosis transmembrane conductance regulator (CFTR) protein has been reported to be associated with chronic pancreatitis (CP). The results remain inconclusive, and therefore, we performed this meta-analysis to clarify the association between M470V and CP risk. Methodology/Results: We conducted a meta-analysis of 7 case-control studies, including a total of 1121 CP patients and 2209 controls from Asian and Caucasian populations. We calculated the odds ratio (OR) and 95% confidence intervals (95% CI). Met470Val was found to be significantly associated with an increased risk of CP under all the genetic models (M vs. V, OR = 1.260, 95% CI: 1.134-1.399; MV vs. VV, OR = 1.292, 95% CI: 1.091-1.530; MM vs. VV, OR = 1.579, 95% CI: 1.274-1.956; MV/MV vs. VV, OR = 1.366, 95% CI: 1.165-1.603; MM vs. MV/VV, OR = 1.346, 95% CI: 1.114-1.621). Met470Val was also found to be significantly associated with an increased risk of idiopathic CP (ICP) in allele contrast, codominant, and recessive models (M vs. V, OR = 1.298, 95% CI: 1.020-1.653; MV vs. VV, OR = 1.297, 95% CI: 1.074-1.566; MM vs. VV, OR = 1.473, 95% CI: 1.165-1.862; MM vs. MV/VV, OR = 1.254, 95% CI: 1.023-1.538). Conclusions: The CFTR 470 M allele is significantly associated with an increased risk of CP in both Asian and Caucasian populations. The CFTR 470 M allele is also significantly associated with risk of ICP.

中文翻译:

囊性纤维化跨膜电导调节剂470 Met等位基因与亚洲和白种人人群患慢性胰腺炎的风险增加相关:一项荟萃分析。

背景:据报道,囊性纤维化跨膜电导调节剂(CFTR)蛋白中的Met470Val多态性(1540A> G [rs213950])与慢性胰腺炎(CP)相关。结果仍然没有定论,因此,我们进行了这项荟萃分析以阐明M470V与CP风险之间的关联。方法/结果:我们对7个病例对照研究进行了荟萃分析,包括来自亚洲和白种人人群的1121名CP患者和2209名对照。我们计算了优势比(OR)和95%置信区间(95%CI)。在所有遗传模型下(M vs.V,OR = 1.260,95%CI:1.134-1.399; MV vs. VV,OR = 1.292,95%CI:1.091),发现Met470Val与CP风险增加显着相关-1.53​​0; MM vs.VV,OR = 1.579,95%CI:1.274-1.956; MV / MV vs.VV,OR = 1.366,95%CI:1.165-1.603;MM vs.MV/VV,OR = 1.346,95%CI:1.114-1.621)。在等位基因对比,显性和隐性模型中,还发现Met470Val与特发性CP(ICP)风险增加显着相关(M vs. V,OR = 1.298,95%CI:1.020-1.653; MV vs. VV, OR = 1.297,95%CI:1.074-1.566; MM vs. VV,OR = 1.473,95%CI:1.165-1.862; MM vs. MV / VV,OR = 1.254,95%CI:1.023-1.53​​8)。结论:CFTR 470 M等位基因与亚洲和高加索人群的CP风险增加显着相关。CFTR 470 M等位基因也与ICP风险显着相关。MV vs.VV,OR = 1.297,95%CI:1.074-1.566;MM vs.VV,OR = 1.473,95%CI:1.165-1.862;MM vs.MV/VV,OR = 1.254,95%CI:1.023-1.53​​8)。结论:CFTR 470 M等位基因与亚洲和高加索人群的CP风险增加显着相关。CFTR 470 M等位基因也与ICP风险显着相关。MV vs.VV,OR = 1.297,95%CI:1.074-1.566;MM vs.VV,OR = 1.473,95%CI:1.165-1.862;MM vs.MV/VV,OR = 1.254,95%CI:1.023-1.53​​8)。结论:CFTR 470 M等位基因与亚洲和高加索人群的CP风险增加显着相关。CFTR 470 M等位基因也与ICP风险显着相关。
更新日期:2020-01-01
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